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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584773Generated: October 31, 2026

5-Bromo-1-benzofuran-7-carbaldehyde → HCID 15428564, compound

https://huagongshe.com/reaction/1584773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-1-benzofuran-7-carbaldehydeHCID 21220840—
Reactant1-methyl-5-(tributylstannyl)-1H-1,2,3-triazoleHCID 22609826—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventTolueneHCID 1140—
SolventSodium BicarbonateHCID 516892—
ProductHCID 15428564HCID 15428564251.5%

Reaction Steps

A mixture of 5-bromo-benzofuran-7-carbaldehyde (0.315 g), 1-methyl-5-tributylstannanyl-1H-[1,2,3]-triazole (0.525 g) and bis(triphenylphosphine)palladium (II) chloride (0.05 g) in toluene (7 ml) was stirred and refluxed under nitrogen for 5 h. The cooled mixture was diluted with 8% sodium bicarbonate (30 ml) and extracted with ethyl acetate (3×25 ml). The combined extracts were dried (MgSO4) and the solvent removed in vacuo to give a yellow solid (0.8 g). Purification by FCC, eluting with ethyl acetate-hexane, then ethyl acetate gave a cream solid, which was crystallised from ethyl acetate to give the title compound as pale green crystals (0.18 g), m.p. 180-2°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935972
Source datasetuspto-grants-1999_08
ORD IDord-b6921322051d43b49cf900e5ded90a2e
Source noteuspto-grants-1999_08